← Return to Living with Parkinson's Disease - Meet others & come say hi

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@hopeful33250

Hello @sallyk and welcome to Mayo Connect! How wonderful that your newly diagnosed friend has someone to support her on this journey with PD. If I could make some suggestions for you, look into PD exercises classes in your area. Most classes are now online because of COVID-19 crisis. Here is a link to the MPF exercises, https://www.parkinsonsmi.org/mpf-programs/exercise-and-movement-activities

If you spend time with her, just turn on the exercises and watch them. Exercise and medicines for PD are the optimal combinations!

You might also see if there are PD support groups. Many now have meetings on Zoom. She can be anonymous by not showing her picture and not participating if that is more comfortable for her. She can learn much from hearing others talk about PD. Youtube also has lots of videos with information about PD as well as exercise classes. Here is a link for those,



I would also like to invite some other members to this discussion including @mariemarie, @ggopher @psvantx, @jdb @susan62. I would encourage you to also read many of the other posts here in this discussion.

What symptoms seem to be the worst for your friend now?

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Replies to "Hello @sallyk and welcome to Mayo Connect! How wonderful that your newly diagnosed friend has someone..."

First, let me send BIG KUDOS to SallyK....what a jewel! Update on me: after being diagnosed with PD and starting researching/reading everything I could find (starting Azilect), etc., I decided to visit a Parkinson’s specialist for second opinion! Glory be, he says I don’t have it and can stop the medicine....music to my ears!!! Praying he is right. He has dealt with only Parkinson’s cases for 25 years. He says lots of afflictions cause the same symptoms....which makes it easy to just diagnose PD.